Reversal of the stereochemical course of the addition of phenylmagnesium bromide to N-benzylimines derived from R-glyceraldehyde depending on the O-protecting group and its application to the synthesis of both enantiomers of phenylglycine
- 1 January 1997
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 53 (4) , 1411-1416
- https://doi.org/10.1016/s0040-4020(96)01053-8
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Stereoselective synthesis of α-hydroxy-β-amino acids using D-glyceraldehyde as the homochiral sourceTetrahedron: Asymmetry, 1996
- Recent Advances in the .beta.-Lactam Synthon MethodAccounts of Chemical Research, 1995
- Recent developments in the stereoselective synthesis of α-aminoacidsTetrahedron, 1994
- 3‐Amino‐2H‐Azirines. Synthons for α,α‐Disubstituted α‐Amino Acids in Heterocycle and Peptide Synthesis [New Analytical Methods (43)]Angewandte Chemie International Edition in English, 1991
- Structure elucidation of the novel glycopeptide antibiotic UK-68,597The Journal of Organic Chemistry, 1990
- Structure of the antibiotic OA-7653The Journal of Organic Chemistry, 1988
- Teicoplanin, antibiotics from Actinoplanes teichomyceticus nov. sp. VIII.Opening of the polypeptide chain of teicoplanin aglycone under hydrolytic conditions.The Journal of Antibiotics, 1987
- Iodination of vancomycin, ristocetin A, and ristocetin pseudoaglyconThe Journal of Organic Chemistry, 1986
- Structural studies on some antibiotics of the vancomycin group, and on the antibiotic-receptor complexes, by proton NMRAccounts of Chemical Research, 1984
- Vancomycin and related antibioticsPharmacology & Therapeutics, 1982